| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40856590-40856751 | Rare:65 | ||||
| chr22:41286168-41286513 | Common:2; Rare:109 | ||||
| chr22:41446778-41446958 | Rare:71 | ||||
| chr22:41468903-41469149 | Rare:67 | ||||
| chr22:41621012-41621370 | Common:7; Rare:133 | ||||
| chr22:41832828-41833149 | Common:3; Rare:102 | ||||
| chr22:41947072-41947204 | Common:1; Rare:48 | ||||
| chr22:42070782-42071060 | Common:3; Rare:60 | ||||
| chr22:42079634-42079763 | Common:1; Rare:38 | ||||
| chr22:42090740-42091007 | Common:1; Rare:95; Clinvar (pathogenic):1 | ||||
| chr22:42614834-42615255 | Common:3; Rare:186 | ||||
| chr22:42649311-42649594 | Common:6; Rare:99 | ||||
| chr22:43089338-43089507 | Common:3; Rare:53 | ||||
| chr22:43812242-43812441 | Common:3; Rare:66 | ||||
| chr22:43955303-43955560 | Common:3; Rare:77 |